Canonical Allele Identifier: CA2696726008

Gene: NRAS

Linked Data

• dbSNP Id: rs2101741720

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713797T>G , CM000663.2:g.114713797T>G	GRCh38
NC_000001.10:g.115256418T>G , CM000663.1:g.115256418T>G	GRCh37
NC_000001.9:g.115057941T>G	NCBI36
NG_007572.1:g.8098A>C , LRG_92:g.8098A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+3A>C MANE Select	ENSP00000358548.4:n.290+3A>C
ENST00000369535.4:c.290+3A>C	ENSP00000358548.4:n.290+3A>C
NM_002524.4:c.290+3A>C	NP_002515.1:n.290+3A>C
NM_002524.5:c.290+3A>C MANE Select	NP_002515.1:n.290+3A>C